HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31860459A>G , CM000668.2:g.31860459A>G | GRCh38 |
NC_000006.11:g.31828236A>G , CM000668.1:g.31828236A>G | GRCh37 |
NC_000006.10:g.31936215A>G | NCBI36 |
NG_008201.1:g.7474T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000375631.5:c.778T>C MANE Select | ENSP00000364782.4:p.Phe260Leu | |
ENST00000677054.1:n.2021T>C | ||
ENST00000677512.1:n.886T>C | ||
ENST00000678869.1:n.1452T>C | ||
ENST00000375631.4:c.778T>C | ENSP00000364782.4:p.Phe260Leu | |
ENST00000480384.1:n.807T>C | ||
ENST00000491768.5:c.778T>C | ENSP00000433127.1:p.Phe260Leu | |
ENST00000495807.1:n.1912T>C | ||
NM_000434.3:c.778T>C | NP_000425.1:p.Phe260Leu | |
NM_000434.4:c.778T>C MANE Select | NP_000425.1:p.Phe260Leu |